Aminophenols
eMolecules Key Organics/BIONET Medetomidine Hydrochloride 8mg 564356417 AS-2748 99 000 86347-15-1 236 740 C13H17ClN2
Key Organics/BIONET Medetomidine Hydrochloride 8mg 564356417 AS-2748 99 000 86347-15-1 236 740 C13H17ClN2
eMolecules Key Organics/BIONET Medetomidine Hydrochloride 1mg 564356411 AS-2748 99 000 86347-15-1 236 740 C13H17ClN2
Key Organics/BIONET Medetomidine Hydrochloride 1mg 564356411 AS-2748 99 000 86347-15-1 236 740 C13H17ClN2
Medchemexpress LLC CGP71683 hydrochloride | 192322-50-2 | MFCD07783999 | 99.4% | 512.07 | C26H30ClN5O2S | 10 MG
CGP71683 hydrochloride is the hydrochloride salt of a selective neuropeptide Y Y5 receptor antagonist used as a research tool in neuroscience and endocrinology. It is supplied as a high-purity solid for non-clinical laboratory use, with supporting datasheet and certificate of analysis available.
- Selective antagonist for the neuropeptide Y Y5 receptor (Ki ~1.3 nM).
- High reported purity, 99.4%.
- Molecular weight 512.07 g/mol; chemical formula C26H30ClN5O2S.
- CAS number 192322-50-2 for unambiguous identification.
- Solid powder suitable for dissolution in appropriate solvents for assays.
- Supplied with datasheet and certificate of analysis for quality assurance.
- Available in small milligram pack sizes for screening and mechanistic studies.
eMolecules Key Organics/BIONET Medetomidine Hydrochloride 2mg 564356412 AS-2748 99 000 86347-15-1 236 740 C13H17ClN2
Key Organics/BIONET Medetomidine Hydrochloride 2mg 564356412 AS-2748 99 000 86347-15-1 236 740 C13H17ClN2
Cayman Chemical Acetaminophen Inhibitors
An analgesic and antipyretic compound; an inhibitor of COX-2 that is selective over COX-1 (IC50s = 113.7 and 25.8 µM, respectively, in human blood ex vivo); induces ferroptotic cell death in primary mouse hepatocytes; has a metabolite that depletes glutathione reserves in the liver
Cayman Chemical NGaminoLArginine hydrochlori
Inhibits nNOS, iNOS, and eNOS (Ki = 0.3, 3, and 2.5 μM, respectively); can be used both in cell culture and in vivo
Chemscene ChemScene | 2,3-Diaminophenol | 10G | CS-W005863 | 0.97 | 59649-56-8| MFCD00075199 | 124.14
ChemScene | 2,3-Diaminophenol | 10G | CS-W005863 | 0.97 | 59649-56-8| MFCD00075199 | 124.14
Medchemexpress LLC RS100329 hydrochloride (2,4(1H,3H)-pyrimidinedione derivative) | 1215654-26-4 | 99.6% | 462.89 | C20H26ClF3N4O3 | 1 ML
RS100329 hydrochloride is a potent, selective α1A-adrenoceptor antagonist provided for in vitro receptor pharmacology and biochemical assays. It is available as a pre-made 10 mM solution in DMSO (1 mL) and in multiple solid sizes, with accompanying analytical documentation for research use.
- Potent, selective α1A-adrenoceptor antagonist suitable for in vitro studies.
- Available as 10 mM DMSO solution (1 mL) and as solid in multiple mg sizes.
- High purity (99.57%) appropriate for biochemical assays.
- Molecular weight 462.89 and formula C20H26ClF3N4O3.
- Supplied with data sheet, certificate of analysis, and safety data sheet.
- Intended for research use; follow laboratory safety and SDS guidance.
Sigma Aldrich Fine Chemicals Biosciences 4-Nitrophenol-2,3,5,6-d4 98 atom % D, 98% (CP) | 93951-79-2 | MFCD00143352 | 250MG
4-Nitrophenol-2,3,5,6-d4 98 atom % D, 98% (CP) | Purity: 98% (CP) | Mol Wt: 143.13 | 93951-79-2 | MFCD00143352 | 250MG
Medchemexpress LLC Ozanimod (hydrochloride) | 1618636-37-5 | 98.1% | 1 ML
Ozanimod hydrochloride 10 mM in DMSO (1 mL) is a ready-to-use research reagent for studying sphingosine 1-phosphate (S1P) receptor modulation in preclinical and biochemical assays. Supplied as a solution to improve handling and reproducibility. For research use only; not for human use.
- Ready-to-use 10 mM solution in DMSO.
- Supplied as a 1 mL aliquot for small-scale experiments.
- Listed purity 98.1% for consistent experimental results.
- Molecular weight 440.92 g/mol and formula C23H25ClN4O3.
- Intended for research use only; not for clinical or human use.
eMolecules 2,4-Dimethyl-6-nitrophenol | 14452-34-7 | MFCD00191633 | 1g
Combi-Blocks, Inc. | 2,4-Dimethyl-6-nitrophenol | 1g | 569292384 | QF-0773 | 95.000 | 14452-34-7 | MFCD00191633 | 167.164 | C8H9NO3
If you are unable to find the chemical you are looking for, make sure you are logged into your fishersci.com account and click on the following link:
eMolecules Building Block Tool
Medchemexpress LLC Hlcl-61 hydrochloride | 1158279-20-9 | MFCD09446681 | 99.9% | 380.91 g·mol⁻¹ | C23H25ClN2O | 100 MG
HLCL-61 hydrochloride is a research-grade small-molecule inhibitor of protein arginine methyltransferase 5 (PRMT5), intended for in vitro and preclinical studies. It is supplied with analytical data and handling guidance and is not for human or clinical use.
- Potent and selective PRMT5 inhibition for cellular studies.
- High chemical purity suitable for research applications.
- Available in multiple pack sizes and ready-to-use DMSO solutions.
- Supplied with supporting datasheet and analytical information.
- Intended for controlled laboratory use with recommended storage conditions.
Apexbio Technology LLC OTS964 hydrochloride 1338545-07-5 2mg
OTS964 hydrochloride (CAS 1338545-07-5) is a selective inhibitor of T-lymphokine-activated killer cell-originated protein kinase (TOPK) demonstrating an IC50 of 28 nM against its target As a dimethylated derivative of OTS514 OTS964 displays high affinity and selectivity for TOPK a serine/threonine kinase implicated in various human malignancies In vitro OTS964 potently suppresses proliferation of multiple TOPK-positive cancer cell lines (IC50 values ranging from 7 6 to 73 nM) while showing markedly reduced activity in TOPK-negative models In in vivo studies OTS964 administered intravenously to mice bearing LU-99 xenografts resulted in significant tumor growth inhibition without notable toxicity Research applications include studying TOPK-related oncogenic pathways and hematopoietic cell differentiation
Medchemexpress LLC Imiloxan hydrochloride | 81167-22-8 | 98.5% | 280.75 g/mol | C14H17ClN2O2 | 5 MG
Imiloxan hydrochloride is a potent, selective α2B-adrenoceptor antagonist used in pharmacological research to probe α2-adrenergic receptor subtype function. It is supplied as a characterized solid with defined purity and molecular weight for use in receptor-binding studies, in vitro assays, and in vivo experiments.
- Selective α2B-adrenoceptor antagonist
- High purity suitable for research applications
- Supplied in small research pack sizes for lab use
- Supported by analytical data (HNMR, LC-MS)
- Provided with SDS, COA, and handling instructions
Selleck Chemical LLC OTS514 hydrochloride-2mg
OTS514 is a highly potent TOPK(T-LAK cell-originated protein kinase) inhibitor with an IC50 value of 2.6 nM. OTS514 induces cell cycle arrest and apoptosis.